Does anyone have any experience with LDN use for a teenager (14) with possible MS? My daughter is experiencing multiple symptoms. She has one lesion on her spine and "time will tell" comments from the doctor. The symptoms come and go, but lately they seem progressing. Please share any experience you may have. I know LDN has been used in autisn and Crohn's in children, but the studies were only 8 weeks long. I am ...

I do have prescription for LDN and have taken it last 3 months but my compound pharmacy charging me $60 for one month supply (3 mg)
do you know of any Pharmacy who can supply the prescription for less and ship it to me?

Thanks in advance

How long where you on LDN before you started feeling the effects good or bad?

Ive been on it for about 3 months 3 mg with no effects

I have been on LDN for about 3 months, but at first was also taking 20 mg/night of amitriptyllne, which is sedating.

I'm working on getting off the amitriptyline, and am now down to 10 mg.

It's been about 2 weeks on the lower dose, and I've found that the vivid dreams that started when I started the LDN have become, well, more vivid and sort of tiring. They aren't nightmares, but hectic, fast-paced and ...

After 7 months on LDN 3mg I had to stop LDN because of increasing severe spasms & intense pain all day & night. I have a baclofen pump that usually controls the pain & spasms but after having numerous tests a dye pumpogram showed that all the baclofen was leaking into the gut through a hole & not going down the spine. (This caused new weakness in left hand/arm which I has taken nearly 4 ...

I have been having some sleep disturbance lately, and headaches (sort of mild, background type), and it reminds me of how I felt when I first started taking LDN two years ago. It seems weird that I'd suddenly be having side effects again after taking it for so long, but that is what this feels like! I'm currently taking 4.5mg and have been at that dose for most of the 2 years (I started at ...

The big news today seems to be that an FDA advisory panel is positive about a new diet drug:

http://online.wsj.com/article/BT-CO-20101208-714967.html

The mention of naltrexone caught my eye:

Hi all,

I have been on Copaxone since October of this year, and have noticed a huge increase in my fatigue.....not sure how common this is, but it is very tough trying to keep up with my 2 little ones. I have been doing a lot of reading into LDN and am wondering how many of you take it along with Copaxone? From what I can tell LDN has helped many with fatigue and brain ...

Lot's of MS testimonials on this...

http://www.youtube.com/user/TheLDNresea ... 1Mqjl0RMeI

Or google...

"LDN Research Trust YouTube Channel"

We need your VOTE today and everyday for the next month because we have applied for a Pepsi Refresh Everything grant to support Non-Mainstream MS Research -- this means that CCSVI (chronic cerebrospinal venous insufficiency), LDN (low dose naltrexone) etc. can be studied using rigorous scientific method.

We are competing against kids who have vast online social networks and we need to vote daily to support MS research. We also need you to send this ...